APOE4、体重变化与长寿有何关系?因果中介分析的启示。

IF 3.3 Q2 GERIATRICS & GERONTOLOGY Frontiers in aging Pub Date : 2024-03-01 eCollection Date: 2024-01-01 DOI:10.3389/fragi.2024.1359202
Rachel Holmes, Hongzhe Duan, Olivia Bagley, Deqing Wu, Yury Loika, Alexander Kulminski, Anatoliy Yashin, Konstantin Arbeev, Svetlana Ukraintseva
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引用次数: 0

摘要

众所周知,APOE 基因的ε4 等位基因(APOE4)与人类的寿命呈负相关,但其机制尚不清楚。APOE4 还与体重变化有关,在一些研究中,体重变化与存活率有关。在此,我们采用因果中介分析(CMA)方法来探索体重的老化变化在 APOE4 与长寿之间的联系中的作用,从而揭示遗传关联的机制。利用健康与退休研究(HRS)数据,我们检验了一个假设,即 APOE4 与 85 岁以上存活率降低之间的关联是否受体重年龄轨迹关键特征的介导,如达到峰值的年龄和之后体重下降的斜率。中介效应通过总效应(TE)、自然间接效应和中介百分比进行评估。同时还报告了受控直接效应和自然直接效应。CMA结果表明,与非携带者相比,APOE4携带者活到85岁及以上的几率要低19%-22%(TE p = 0.020-0.039),部分原因是他们在较年轻时就达到了体重峰值,之后体重下降得更快。这一发现与 APOE4 对长寿的不利影响部分与 ε4 携带者加速身体衰老有关的观点一致。
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How are APOE4, changes in body weight, and longevity related? Insights from a causal mediation analysis.

The ε4 allele of the APOE gene (APOE4) is known for its negative association with human longevity; however, the mechanism is unclear. APOE4 is also linked to changes in body weight, and the latter changes were associated with survival in some studies. Here, we explore the role of aging changes in weight in the connection between APOE4 and longevity using the causal mediation analysis (CMA) approach to uncover the mechanisms of genetic associations. Using the Health and Retirement Study (HRS) data, we tested a hypothesis of whether the association of APOE4 with reduced survival to age 85+ is mediated by key characteristics of age trajectories of weight, such as the age at reaching peak values and the slope of the decline in weight afterward. Mediation effects were evaluated by the total effect (TE), natural indirect effect, and percentage mediated. The controlled direct effect and natural direct effect are also reported. The CMA results suggest that APOE4 carriers have 19%-22% (TE p = 0.020-0.039) lower chances of surviving to age 85 and beyond, in part, because they reach peak values of weight at younger ages, and their weight declines faster afterward compared to non-carriers. This finding is in line with the idea that the detrimental effect of APOE4 on longevity is, in part, related to the accelerated physical aging of ε4 carriers.

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